Medication info

Uniphezil Dispersible Tablet 10mg (Donepezil Hydrochloride Hydrate)

Prescription medicationOrally disintegrating Tablet경구Expired
Ingredient · strength
Donepezil Hydrochloride Hydrate›10.43mg / 1 tablet
Manufacturer / importer
구주제약(주)
Appearance
Yellow round orally disintegrating tablet
Packaging
30 tablets (10 tablets in PTP packaging × 3)
Approval status
Expired

MFDS item code 201905571 · Approved 2019.08.07

This product's status changed to Expired on 2024.08.07. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of symptoms of Alzheimer-type dementia
Who takes it
Adults · Children
Adult dose
As donepezil hydrochloride, administer 5 mg once daily before bedtime. For 4-6 weeks, the dosage of 5 mg should be administered. After evaluating clinical response, it may be increased to 10 mg. If increasing to a daily dosage of 10 mg, administer while being cautious of gastrointestinal side effects. This medication is an orally disintegrating tablet that can be placed on the tongue and dissolved for oral administration without water.
Child dose
No experience in pediatric use.

Ingredients

Manufacturer
구주제약(주)

Efficacy & effects

Improvement of symptoms of Alzheimer-type dementia

  • Symptoms of Alzheimer-type dementia
View approved original text

This medication is used for the treatment of symptoms of Alzheimer-type dementia. Alzheimer-type dementia presents symptoms like memory decline and cognitive dysfunction, and this medication helps alleviate these symptoms and improve the patient's functional living abilities.

How to take

Adult dose

As donepezil hydrochloride, administer 5 mg once daily before bedtime. For 4-6 weeks, the dosage of 5 mg should be administered. After evaluating clinical response, it may be increased to 10 mg. If increasing to a daily dosage of 10 mg, administer while being cautious of gastrointestinal side effects. This medication is an orally disintegrating tablet that can be placed on the tongue and dissolved for oral administration without water.

Child dose

No experience in pediatric use.

Precautions

This medication contains the artificial sweetener aspartame, so it should not be used by patients with the genetic condition phenylketonuria. Patients with hypersensitivity to this medication, pregnant women, or nursing mothers should avoid taking it. Patients with certain diseases such as heart disease, peptic ulcer, asthma, or Parkinson's disease should be particularly cautious when using this medication. This medication may affect heart rate, so patients with poor heart health should take it under medical supervision. Serious side effects such as gastrointestinal bleeding, liver dysfunction, and cerebrovascular problems may occur, so consult a healthcare professional immediately if symptoms appear. While taking this medication, care should be taken as neurological side effects such as dizziness, drowsiness, insomnia, and hallucinations may occur. This medication may affect the ability to drive or operate machinery, so extra caution is needed during initial usage or dosage changes. There may be interactions with other medications, so patients currently taking other medications must inform their healthcare provider. If pregnant or nursing, avoid using this medication or consult with a specialist if absolutely necessary. Safety for pediatric use has not been established, so it is generally advised not to use it in children. In case of overdose, symptoms such as severe nausea, vomiting, or breathing difficulties may occur, requiring immediate medical attention. This medication is taken by dissolving it in the mouth, so it is important to follow the administration instructions accurately and keep it out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in oral/eye mucosa, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of the skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urination issues

Mild side effects

  • Nausea
  • vomiting
  • diarrhea
  • loss of appetite
  • headache
  • fatigue
  • drowsiness
  • insomnia
  • dizziness
  • muscle pain
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  • rash
  • itching
  • urinary incontinence
  • frequent urination
  • fever
  • decreased body temperature
  • dehydration
  • hyperlipidemia
  • hypokalemia
  • hypoglycemia
  • weight gain
  • thrombocytopenia
  • anemia
  • blood abnormalities
  • palpitations
  • hypertension
  • hypotension
  • atrial fibrillation
  • heart failure
  • myocardial infarction
  • sinoatrial block
  • atrioventricular block
  • musculoskeletal abnormalities
  • anxiety
  • mania
  • hallucinations

Not everyone experiences these, and they can vary from person to person.

Storage

Store this medication in a tightly sealed container that allows for good air circulation, and keep it at room temperature between 1 degree Celsius and 30 degrees Celsius. Storing it this way can help maintain the medication's effectiveness for a longer time.

Appearance and packaging

Appearance

Yellow round orally disintegrating tablet

Package unit

30 tablets (10 tablets in PTP packaging × 3)

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.